CHANGES IN AGGRESSIVE AND SEXUAL RESPONSIVENESS OF MALE GOLDEN HAMSTERS AFTER NEONATAL ANDROGEN ADMINISTRATION

1977 ◽  
Vol 73 (2) ◽  
pp. 331-337 ◽  
Author(s):  
A. P. PAYNE

SUMMARY On day 1 after birth, male golden hamsters received either 300 μg of an androgen (testosterone propionate, testosterone, dihydrotestosterone or androstenedione) in 0·03 ml arachis oil, or oil alone. As intact adults, their aggressiveness towards unreceptive females was measured. After this, all animals were castrated. At least 3 weeks after the operation all animals received oestradiol benzoate (10 μg + progesterone (500 μg), after which their capacity to show patterns of female sexual behaviour towards a stud male was tested. Control hamsters which had received oil as neonates showed less aggression than the females with which they interacted; these controls also readily assumed lordosis after castration and priming with ovarian steroids. Conversely, animals which had received testosterone propionate or androstenedione neonatally were as aggressive as the female hamsters, and showed a markedly decreased ability to display lordotic behaviour after castration. The behaviour of male hamsters which received testosterone or dihydrotestosterone was unaffected. Thus, at the level of treatment used, increased aggressiveness appeared to co-vary with a decreased capacity to show female sexual behaviour patterns. However, within each treatment there was little evidence of such a relationship at the level of the individual animal.

1976 ◽  
Vol 69 (1) ◽  
pp. 23-31 ◽  
Author(s):  
A. P. PAYNE

SUMMARY Female golden hamsters received one of the following treatments on the day following birth: (i) 300 μg testosterone propionate in arachis oil, (ii) 300 μg testosterone in oil, (iii) 300 μg dihydrotestosterone in oil, or (iv) oil alone. As adults all animals underwent three tests for behaviour. First, while intact, females were observed in aggressive interactions with males. Secondly, after ovariectomy, females were primed with oestrogen + progesterone and tested for receptivity with a stud male. Thirdly, all ovariectomized females were primed with testosterone propionate and tested for male patterns of behaviour with a receptive female. Compared with the effects of oil administration (control), testosterone propionate administration resulted in increased aggressiveness and the capacity to show male patterns of sexual behaviour, together with a decreased capacity to show female patterns of sexual behaviour. Testosterone increased aggression and male sexual behaviour, but had no effects on receptivity, while dihydrotestosterone decreased some components of receptivity but had no effects on aggressiveness or the capacity to show male mating behaviour.


1978 ◽  
Vol 79 (1) ◽  
pp. 69-76 ◽  
Author(s):  
JANET E. BOOTH

Groups of rats were castrated on the day of birth (day 1) and injected with testosterone, androst-4-ene-3,6,17-trione (ADT, an inhibitor of aromatization), testosterone + ADT or oil daily from day 1 to day 5. The aromatizable androgen testosterone suppressed both cyclic gonadotrophin secretion, as judged from the absence of corpora lutea in grafted ovaries, and the behavioural response to injections of oestradiol benzoate and progesterone in adulthood. It also stimulated normal development of the penis and ejaculation in behaviour tests carried out after injections of testosterone propionate. The aromatization inhibitor ADT, like oil, did not affect either cyclic gonadotrophin secretion or receptive behaviour, but injections of ADT given at the same time as testosterone significantly reduced the effects of the androgen on both cyclic gonadotrophin secretion and receptive behaviour. Although neonatal administration of ADT did not affect the testosterone-stimulated development of the penis or the ability of the rats to achieve penile intromissions, it did interfere with ejaculation. None of the rats which had been injected with testosterone+ADT ejaculated. These results support the concept that during infancy neural conversion of androgens to oestrogens is important both for the suppression of the female patterns of gonadotrophin secretion and sexual behaviour and for the central organization of normal patterns of male sexual behaviour. Normal completion of the differentiation of the male genital tract appears to be independent of the central organization of masculine patterns of sexual behaviour.


1981 ◽  
Vol 90 (1) ◽  
pp. 97-102 ◽  
Author(s):  
A. BARTKE ◽  
H. KLEMCKE ◽  
A. AMADOR

Testicular regression was induced in adult golden hamsters by exposure to a short photoperiod (5 h light: 19 h darkness). The response of these animals to exogenous steroids (ten injections each of 5 mg testosterone, testosterone propionate, pregnenolone, progesterone or cortisol administered s.c. three times/week) was evaluated from weight changes in testes and seminal vesicles, from plasma levels of LH, FSH and testosterone, and from testicular human chorionic gonadotrophin (HCG) binding and testosterone levels. Administration of testosterone or testosterone propionate produced a decrease in plasma gonadotrophins and a three- to fourfold increase in weights of testes and seminal vesicles, thus indicating that the seminiferous tubules, similarly to accessory reproductive glands, retained the ability to respond to androgenic stimulation. Binding of HCG by testicular tissue was dramatically reduced by treatment with testosterone, probably reflecting atrophy of the Leydig cells. Treatment with pregnenolone or progesterone failed to increase testicular weight, seminal vesicle weight or concentrations of testosterone in the testes. This suggests that the atrophic testes of these animals may have a limited capacity to produce biologically significant amounts of androgens from C21 steroids. Administration of cortisol did not alter any of the parameters of reproductive function that were examined.


1973 ◽  
Vol 58 (3) ◽  
pp. 627-636 ◽  
Author(s):  
A. P. PAYNE ◽  
H. H. SWANSON

SUMMARY Male golden hamsters received either 300 μg testosterone propionate or oil on day 1 of life. As adults they were observed (i) when intact (ii) when castrated and (iii) when receiving 1 mg testosterone propionate per day in interactions with intact dioestrous females. Male controls which had received oil neonatally resembled normal untreated males in showing less aggressive behaviour than females. Castration and subsequent androgen administration did not affect aggression in the controls. Conversely, neonatally androgenized males showed comparable levels of aggression to the females with which they interacted. Castration reduced aggressive behaviour in these males, while subsequent androgen administration resulted in them showing significantly more aggression than females. In particular, when intact or receiving androgen replacement, neonatally androgenized males attacked and bit females, a behaviour seldom seen in normal males or in those given oil neonatally. Sexual investigation and following decreased in both groups of males after castration, and increased under androgen replacement. These changes were more pronounced in the neonatally androgenized males, indicating a greater behavioural responsiveness to androgens in this group. It is suggested that the behaviour of the normal male hamster is incompletely 'masculinized' during neonatal development, and the possible adaptive significance of this is discussed.


1971 ◽  
Vol 51 (4) ◽  
pp. 615-620 ◽  
Author(s):  
LEONORE TIEFER ◽  
W. A. JOHNSON

SUMMARY Four groups of adult male hamsters were castrated and injected with either 6 μg oestradiol benzoate (OB), 100 μg OB, 6 μg OB plus 0·5 mg progesterone or 100 μg OB plus 0·5 mg progesterone. In repeated tests with virile males, all the injected males showed lordosis behaviour similar, but quantitatively inferior, to that of female hamsters. Uninjected controls showed no lordosis. There was no dose—response relationship between the two doses of oestrogen. Progesterone significantly facilitated the quantity and quality of lordosis behaviour shown. This is in contrast with previous reports of the absence of facilitation by progesterone in male rats. After cessation of hormone injections the animals continued to display the lordosis response for several weeks.


1966 ◽  
Vol 52 (3) ◽  
pp. 471-477 ◽  
Author(s):  
G. P. van Rees ◽  
E. Gans

ABSTRACT In female rats sterilized by an injection of testosterone propionate (TP) shortly after birth, the effects of gonadectomy and gonadectomy plus chronic treatment with oestradiol benzoate were studied. Pituitary LH-contents were affected in a similar way as in normal females, although there was an indication that the sensitivity of the response of pituitary LH-content to oestradiol was slightly less in TP-sterilized than in normal rats. The effect of oestradiol on uterine weights was definitely less in gonadectomized TP-sterilized rats than in gonadectomized controls. It was therefore concluded that negative feedback mechanisms between ovarian steroids and LH-secretion operate in a normal manner in TP-sterilized rats. The sensitivity of the uterus to oestrogen, however, is decreased.


1977 ◽  
Vol 75 (3) ◽  
pp. 383-389 ◽  
Author(s):  
L. G. CLEMENS ◽  
B. A. GLADUE

Intracerebral infusion of prostaglandin E2 (PGE2) facilitated copulatory behaviour of longterm castrated rats. Castrated rats were given daily systemic injections of testosterone propionate (50 pg) or oil vehicle, and then 30 min before behavioural testing they received an intrahypothalamic infusion of either PGE2 or saline. Rats receiving PGE2 in addition to systemic testosterone showed more copulatory behaviour than those receiving PGE2 or testosterone alone.


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